首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Quantitative determination of hydroxy polycylic aromatic hydrocarbons as a biomarker of exposure to carcinogenic polycyclic aromatic hydrocarbons
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Quantitative determination of hydroxy polycylic aromatic hydrocarbons as a biomarker of exposure to carcinogenic polycyclic aromatic hydrocarbons

机译:定量测定羟基多环芳烃作为暴露于致癌多环芳烃的生物标志物

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A high-resolution gas chromatography/high-resolution mass spectrometry (HRGC/HRMS) method was developed for quantitative analysis of hydroxy polycyclic aromatic hydrocarbons (OH-PAHs). Four hydroxy metabolites of known and suspected carcinogenic PAHs (benzo[a]pyrene (B[a]P), benz[a]anthracene (B[a]A), and chrysene (CRY)) were selected as suitable biomarkers of PAH exposure and associated risks to human health. The analytical method included enzymatic deconjugation, liquid - liquid extraction, followed by derivatization with methyl-N-(trimethylsilyl) trifluoroacetamide and instrumental analysis. Photo-induced oxidation of target analytes - which has plagued previously published methods - was controlled by a combination of minimizing exposure to light, employing an antioxidant (2-mercaptoethanol) and utilizing a nitrogen atmosphere. Stability investigations also indicated that conjugated forms of the analytes are more stable than the non-conjugated forms. Accuracy and precision of the method were 77.4-101% (<4.9% RSD) in synthetic urine and 92.3-117% (<15% RSD) in human urine, respectively. Method detection limits, determined using eight replicates of low-level spiked human urine, ranged from 13 to 24 pg/mL. The method was successfully applied for analysis of a pooled human urine sample and 78 mouse urine samples collected from mice fed with PAH-contaminated diets. In mouse urine, greater than 94% of each analyte was present in its conjugated form. (C) 2016 Elsevier B.V. All rights reserved.
机译:建立了高分辨率气相色谱/高分辨率质谱(HRGC / HRMS)方法,用于定量分析羟基多环芳烃(OH-PAHs)。选择四种已知和疑似致癌PAHs的羟基代谢物(苯并[a]((B [a] P),苯并[a]蒽(B [a] A)和,(CRY)))作为PAH暴露的合适生物标志物以及对人类健康的相关风险。分析方法包括酶解偶联,液-液萃取,然后用甲基-N-(三甲基甲硅烷基)三氟乙酰胺衍生化和仪器分析。目标分析物的光诱导氧化-困扰着先前发表的方法-是通过以下两种方法来控制的:将曝光最小化,使用抗氧化剂(2-巯基乙醇)和利用氮气气氛。稳定性研究还表明,分析物的结合形式比非结合形式更稳定。该方法在合成尿中的准确度和精密度分别为77.4-101%(RSD <4.9%)和人尿中92.3-117%(RSD <15%)。方法检测限由13次低浓度加标的人类尿液重复测定,范围为13至24 pg / mL。该方法已成功地用于分析合并的人类尿液样本和从受PAH污染饮食喂养的小鼠中收集的78种小鼠尿液样本。在小鼠尿液中,超过94%的每种分析物都以其结合形式存在。 (C)2016 Elsevier B.V.保留所有权利。

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